ANKRD26, ankyrin repeat domain 26, 22852

N. diseases: 41; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10764671
rs10764671 		10 27095178 intron variant T/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs10829163
rs10829163 		10 27028911 missense variant C/T snv 0.22 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971 		10 27068541 intron variant A/C;G snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2019 2019
dbSNP: rs7081476
rs7081476 		0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7081476
rs7081476 		0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7081476
rs7081476 		0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs7081476
rs7081476 		0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7081476
rs7081476 		0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7081476
rs7081476 		0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7081476
rs7081476 		0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs863223318
rs863223318 		1.000 0.120 10 27100460 5 prime UTR variant C/T snv
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		Hemic and Lymphatic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1554800065
rs1554800065 		1.000 0.120 10 27100445 5 prime UTR variant G/C snv
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1554800065
rs1554800065 		1.000 0.120 10 27100445 5 prime UTR variant G/C snv
CUI: C1861185
Disease: THROMBOCYTOPENIA 2 (disorder)
THROMBOCYTOPENIA 2 (disorder) 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 0